Canonical Allele Identifier: CA2187827296

Gene: CYP1A2

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.74755350_74755354delinsCAAAA , CM000677.2:g.74755350_74755354delinsCAAAA	GRCh38
NC_000015.9:g.75047691_75047695delinsCAAAA , CM000677.1:g.75047691_75047695delinsCAAAA	GRCh37
NC_000015.8:g.72834744_72834748delinsCAAAA	NCBI36
NG_008431.1:g.37809_37813delinsCAAAA
NG_008431.2:g.37809_37813delinsCAAAA
NG_061543.1:g.11506_11510delinsCAAAA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000343932.5:c.*262_*266delinsCAAAA MANE Select	ENSP00000342007.4:n.*262_*266delinsCAAAA
ENST00000343932.4:c.*262_*266delinsCAAAA	ENSP00000342007.4:n.*262_*266delinsCAAAA
NM_000761.4:c.*262_*266delinsCAAAA	NP_000752.2:n.*262_*266delinsCAAAA
NM_000761.5:c.*262_*266delinsCAAAA MANE Select	NP_000752.2:n.*262_*266delinsCAAAA